Skip to main content
. 2009 Jun 15;3:7225. doi: 10.4076/1752-1947-3-7225

Figure 2.

Figure 2.

(a) Sequence around codon 248 of TP53 showing the mutated base which determines an arginine to tryptophan substitution. (b) The PTEN point mutation at the intron 2 splice donor site causes a defective splicing which likely results in a non-functional protein.